The 2.0 version of rSNPBase

Variant report

Variant rs11799419
Chromosome Location chr1:172913564-172913565
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172903600-172914200 Weak transcription Aorta Aorta
2 chr1:172905600-172916000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr1:172910800-172914200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr1:172910800-172916200 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr1:172911000-172914400 Weak transcription Placenta Amnion Placenta Amnion
6 chr1:172911200-172914200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
7 chr1:172911200-172914400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr1:172911200-172915800 Weak transcription NHDF-Ad bronchial
9 chr1:172911200-172916000 Weak transcription HSMMtube muscle
10 chr1:172911200-172916200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
11 chr1:172911200-172917000 Weak transcription Fetal Stomach stomach
12 chr1:172911200-172917600 Weak transcription Fetal Lung lung
13 chr1:172911400-172916000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr1:172911400-172916000 Weak transcription NH-A brain

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Last update: Aug 31, 2015